Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023 + Amd 1:2025); German version EN ISO 10993-17:2023 + A1:2025

Standard [AVAILABLE PRE-PUBLICATION]

DIN EN ISO 10993-17:2026-05

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023 + Amd 1:2025); German version EN ISO 10993-17:2023 + A1:2025

German title
Biologische Beurteilung von Medizinprodukten - Teil 17: Toxikologische Risikobewertung von Medizinproduktbestandteilen (ISO 10993-17:2023 + Amd 1:2025); Deutsche Fassung EN ISO 10993-17:2023 + A1:2025
Publication date
2026-05
Original language
German
Pages
94

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Publication date
2026-05
Original language
German
Pages
94
DOI
https://dx.doi.org/10.31030/3668043
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Content

ICS

11.100.20

DOI

https://dx.doi.org/10.31030/3668043
Replacement amendments

This document replaces DIN EN ISO 10993-17:2024-02 .

And replaced by 2026-05 for:: DIN EN ISO 10993-17/A1:2024-09 , DIN EN ISO 10993-17:2024-02 .

Document timeline
PRE-PUBLISHED
2026-05

Standard [AVAILABLE PRE-PUBLICATION]

DIN EN ISO 10993-17:2026-05
Drafts
2024-09 - 2026-05

Draft standard

DIN EN ISO 10993-17/A1:2024-09
intended to be withdrawn
2024-02 - 2026-05

Standard

DIN EN ISO 10993-17:2024-02

Cooperation at DIN

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